Job ID R-503087 Date posted October 22, 2024

Be part of something bigger at BD. Here, you’ll help us maintain our high standards from a regulatory perspective at all levels, with a keen focus on submissions. It requires acute attention to detail, excellent communication skills and a passion to keep learning and updating your knowledge, which we’ll help you do with regular learning opportunities. Here, you’ll use your in-depth knowledge of FDA, Canadian and ISO/MDD regulations and requirements surrounding medical devices to ultimately achieve a singular goal: advancing the world of health™. At BD, you can make a true difference of one.

  • Job Type:
    Full-Time
  • Job Level:
    Entry to Senior
  • Travel:
    Varies
  • Salary:
    Competitive
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Responsibilities

Job Description Summary

Job Description

We are the makers of possible!

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us.

In BD – Specimen Management (BD SM), we develop some of the most widely used products in the field of specimen collection including acquisition of the sample, collection into an appropriate container, and emerging point-of-care applications.  Our team has the unique opportunity to be involved with both medical devices and in vitro diagnostics. 

Program Overview:

BD’s Regulatory Affairs internship position is designed to attract highly motivated undergraduate students who want to acquire practical work experience relevant to a career in Regulatory Affairs (RA). As a summer intern, you can expect to add real value to key projects through challenging and exciting work. You will work directly with a manager in your day-to-day role and be assigned mentors to aid and assist you in your transition into the corporate environment. As part of the broader BD Summer Internship Program, interns participate in various networking, career development, and team-building activities!

Throughout your summer internship, you will build an extensive professional network, learn how to work in a regulated environment, build your understanding of the importance of documentation, and deliver on regulatory excellence.

We are recruiting for highly driven students pursuing education in scientific, engineering, or related fields with a passion for innovation, product development and working in the medical device industry.  

Essential / Key Job Responsibilities:

The RA Intern provides support for Regulatory Affairs activities related to global registrations or RA operation projects. The RA Intern may support multiple Regulatory Affairs professionals across different product lines and may work on a single project or support multiple smaller projects. They will assist members of the RA team to support compliance with global regulatory requirements and ensure project and department deliverables are met.  

  • Provide general RA support for regulatory projects, under the direction of an RA professional.  
  • Effectively manage multiple competing priorities and work in a regulated environment. 
  • Assist with the collection of project related documentation and assist with preparation of regulatory submissions. 
  • Work across full suite of Microsoft office software programs, Adobe, and multiple internal software programs/databases. 

Required qualifications:

  • Completion of Junior year pursuing a bachelor’s degree in Biomedical Engineering, Biology, Biochemistry, Microbiology, Biotechnology, Public Health, International Business, Business, Writing & Rhetoric, or a related field
  • Excellent written and oral communication skills   
  • Critical thinker
  • Ability to quickly adapt to new professional collaborative environments, deal with ambiguity, take initiative, and achieve results 
  • Detail oriented 
  • Interest in medical and in vitro diagnostic devices
  • Must be legally authorized to work in the United States without restriction as to duration. 
  • Available to start internship on Monday, June 2, 2025

A mobility stipend is provided.

For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.   

Why Join Us?

A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day.   

You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time. And through the organization’s investment in BD University, you will continually level up your tech skills and expertise.   

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.    

To learn more about BD visit https://bd.com/careers

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.   

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Success Profile

What makes a successful Regulatory Affairs Professional at BD? Check out the top traits we’re looking for and see if you have the right mix.

  • Analytical
  • Collaborative
  • Communicator
  • Persuasive
  • Problem-solver
  • Skilled presenter

Advancing the world of health™

BD is one of the largest global medical technology companies in the world and is advancing the world of health™ by improving medical discovery, diagnostics and the delivery of care. BD helps customers enhance outcomes, lower costs, increase efficiencies, improve safety and expand access to health care.

At BD, we are committed to global inclusion and diversity. Increased inclusion and diversity drives innovation, allows us to better understand patient and customer needs, and ultimately makes BD the best possible place for all associates to thrive.


Brian Carney
Staff Regulatory Affairs Specialist

I love working with high powered leaders on a day to day basis who are respectful to my opinion and who I was never exposed to in my past job.


Robin Cassell
Global Regulatory Operations Labeling Specialist

I have been trusted in my ability to lead exciting and challenging projects with excellent upper management support. This in-turn has allowed me to grow and expand my regulatory knowledge that I believe will lay as a foundation to build my Regulatory career on.


Nikita A Mahendra Kumar
Senior Regulatory Affairs Specialist

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